| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221268-113221597 | Rare:100 | ||||
| chr9:113275392-113275708 | Common:5; Rare:99; Clinvar (pathogenic):1 | ||||
| chr9:113410394-113410705 | Common:2; Rare:78 | ||||
| chr9:120793381-120793534 | Rare:55 | ||||
| chr9:120842916-120843083 | Common:1; Rare:55 | ||||
| chr9:121074860-121074938 | Rare:39 | ||||
| chr9:121268043-121268198 | Common:1; Rare:55 | ||||
| chr9:122264785-122264909 | Common:2; Rare:39 | ||||
| chr9:125241317-125241667 | Common:2; Rare:103 | ||||
| chr9:125707192-125707364 | Common:2; Rare:52 | ||||
| chr9:127451335-127451523 | Common:2; Rare:80 | ||||
| chr9:128160008-128160344 | Common:2; Rare:73 | ||||
| chr9:128275941-128276307 | Common:5; Rare:171 | ||||
| chr9:128322414-128322485 | Rare:27 | ||||
| chr9:128322760-128322861 | Common:2; Rare:42; Clinvar (benign):5 |